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1 February 2007 Multiple Pathways for Cationic Amino Acid Transport in Rat Seminiferous Tubule Cells
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Abstract

Arginine and ornithine are known to be important for various biological processes in the testis, but the delivery of extracellular cationic amino acids to the seminiferous tubule cells remains poorly understood. We investigated the activity and expression of cationic amino acid transporters in isolated rat Sertoli cells, peritubular cells, pachytene spermatocytes, and early spermatids. We assessed the l-arginine uptake kinetics, Na dependence of transport, profiles of cis inhibition of uptake by cationic and neutral amino acids, and sensitivity to trans stimulation of cationic amino acid transporters, and studied the expression of the genes encoding them by RT-PCR. Our data suggest that l-arginine is taken up by Sertoli cells and peritubular cells, principally via system y L (SLC3A2/SLC7A6) and system y (SLC7A1 and SLC7A2), with system B0 making a minor contribution. By contrast, system B0 , associated with system y L (SLC3A2/SLC7A7 and SLC7A6), made a major contribution to the transport of cationic amino acids in pachytene spermatocytes and early spermatids. Sertoli cells had higher rates of l-arginine transport than the other seminiferous tubule cells. This high efficiency of arginine transport in Sertoli cells and the properties of the y L system predominating in these cells strongly suggest that Sertoli cells play a key role in supplying germ cells with l-arginine and other cationic amino acids. Furthermore, whereas cytokines induce nitric oxide (NO) production in peritubular and Sertoli cells, little or no upregulation of arginine transport by cytokines was observed in these cells. Thus, NO synthesis does not depend on the stimulation of arginine transport in these somatic tubular cells.

Virginie Cérec, Claire Piquet-Pellorce, Hamdy A. A. Aly, Anne-Marie Touzalin, Bernard Jégou, and Françoise Bauché "Multiple Pathways for Cationic Amino Acid Transport in Rat Seminiferous Tubule Cells," Biology of Reproduction 76(2), 241-249, (1 February 2007). https://doi.org/10.1095/biolreprod.106.056168
Received: 3 August 2006; Accepted: 1 October 2006; Published: 1 February 2007
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